Entity Details
| Primary name |
KREM1_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q96MU8 |
| EntryName | KREM1_HUMAN |
| FullName | Kremen protein 1 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 473 |
| SequenceStatus | complete |
| DateCreated | 2002-05-15 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell membrane |
Domains
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| Domain | Name | Category | Type |
| IPR000001 | Kringle | Domain | Domain |
| IPR000859 | CUB domain | Domain | Domain |
| IPR002889 | Carbohydrate-binding WSC | Domain | Domain |
| IPR013806 | Kringle-like fold | Family | Homologous superfamily |
| IPR017076 | Kremen | Family | Family |
| IPR018056 | Kringle, conserved site | Site | Conserved site |
| IPR035914 | Spermadhesin, CUB domain superfamily | Family | Homologous superfamily |
| IPR038178 | Kringle superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 617392 | OMIM | Ectodermal dysplasia 13, hair/tooth type (ECTD13) | A form of ectodermal dysplasia, a disorder due to abnormal development of two or more ectodermal structures. ECTD13 is an autosomal recessive form characterized by severe oligodontia accompanied by anomalies of hair and skin. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions